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异源初免-加强型 HIV-1 疫苗诱导的抗正痘病毒中和抗体对插入特异性免疫应答的影响。

Impact of anti-orthopoxvirus neutralizing antibodies induced by a heterologous prime-boost HIV-1 vaccine on insert-specific immune responses.

机构信息

Division of Infectious Diseases, Brigham and Women's Hospital, Boston, MA 02115, United States.

出版信息

Vaccine. 2012 Dec 17;31(1):114-9. doi: 10.1016/j.vaccine.2012.10.093. Epub 2012 Nov 7.

Abstract

BACKGROUND

The impact of anti-vector immunity on the elicitation of insert-specific immune responses is important to understand in vaccine development. HVTN 055 was a 150 person phase I randomized, controlled HIV vaccine trial of recombinant modified vaccinia Ankara (rMVA) and fowlpox (rFPV) with matched HIV-1 inserts which demonstrated increased CD8+ T-cell immune responses in the heterologous vaccine group. The controls used in this study were the empty vectors (MVA and FPV).

METHODS

Anti-MVA and anti-vaccinia neutralizing antibodies (NAbs) were measured and compared with cellular and humoral HIV-1-specific immune responses.

RESULTS

Elicitation of anti-vector responses increased with increasing dose of MVA and up to 2 administrations. Further inoculations of MVA (up to 5) did not increase the magnitude of the anti-MVA response but did delay the anti-vector NAb titre decay. There was no evidence that the insert impaired the anti-vector response, nor that anti-vector immunity attenuated the insert-specific responses.

CONCLUSION

Two doses of MVA may be ideal for the elicitation of orthopoxvirus immune responses with further doses maintaining increased titres against the vector. We found no evidence that eliciting HIV insert- or MVA vector-specific immune responses interfered with elicitation of immune responses to the other.

摘要

背景

在疫苗开发中,了解抗载体免疫对插入特异性免疫反应的影响非常重要。HVTN 055 是一项 150 人的 I 期随机对照 HIV 疫苗试验,使用重组改良安卡拉痘苗(rMVA)和禽痘(rFPV)以及匹配的 HIV-1 插入物,该试验显示在异源疫苗组中 CD8+ T 细胞免疫反应增加。本研究中的对照使用的是空载体(MVA 和 FPV)。

方法

测量抗 MVA 和抗痘苗中和抗体(NAb),并与细胞和体液 HIV-1 特异性免疫反应进行比较。

结果

随着 MVA 剂量的增加和接种次数的增加,抗载体反应增加。进一步接种 MVA(多达 5 次)不会增加抗 MVA 反应的幅度,但会延迟抗载体 NAb 滴度的下降。没有证据表明插入物会损害抗载体反应,也没有证据表明抗载体免疫会减弱插入特异性反应。

结论

两剂 MVA 可能是诱导正痘病毒免疫反应的理想选择,进一步接种可维持对载体的高滴度。我们没有发现诱导 HIV 插入物或 MVA 载体特异性免疫反应会干扰对另一种免疫反应的诱导。

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